Pyrolysis and GC in polymer analysis/ by Levy, E. J., Liebman, S. A.

Mechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiency by Peretti N, Marcil V, Drouin E, Levy E

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Energy Conversion Research by Brown, G. A., Levy, E. K., Kerrebrock, J. L.

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Assembly reflects evolution of protein complexes. by Levy, E, Boeri Erba, E, Robinson, C, Teichmann, SA

Genomic organization of the human galpha14 and Galphaq genes and mutation analysis in chorea-acanthocytosis (CHAC). by Rubio, J, Levy, E, Dobson-Stone, C, Monaco, A

Klinefelter-like phenotype and primary infertility in a male with a paracentric Xq inversion. by Németh, A, Gallen, I, Crocker, M, Levy, E, Maher, E

Functional complementation of a genetic deficiency with human artificial chromosomes. by Mejía, J, Willmott, A, Levy, E, Earnshaw, W, Larin, Z

A Golgi localization signal identified in the Menkes recombinant protein. by Francis, M, Jones, E, Levy, E, Ponnambalam, S, Chelly, J, Monaco, A

Identification of a di-leucine motif within the C terminus domain of the Menkes disease protein that mediates endocytosis from the plasma membrane. by Francis, M, Jones, E, Levy, E, Martin, R, Ponnambalam, S, Monaco, A

Energy Conversion Research by Brown, G. A., Levy, E. K., Hoffman, M. A., Zeiders, G. W.

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Characterisation of X;17(q12;p13) translocation breakpoints in a female patient with hypomelanosis of Ito and choroid plexus papilloma. by Zajac, V, Kirchhoff, T, Levy, E, Horsley, S, Miller, A, Steichen-Gersdorf, E, Monaco, A

The human 2',5'-oligoadenylate synthetase locus is composed of three distinct genes clustered on chromosome 12q24.2 encoding the 100-, 69-, and 40-kDa forms. by Hovnanian, A, Rebouillat, D, Mattei, MG, Levy, E, Marié, I, Monaco, A, Hovanessian, A

Efficiency of de novo centromere formation in human artificial chromosomes. by Mejía, J, Alazami, A, Willmott, A, Marschall, P, Levy, E, Earnshaw, W, Larin, Z

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region. by Bonora, E, Bacchelli, E, Levy, E, Blasi, F, Marlow, A, Monaco, A, Maestrini, E

X-linked recessive hypoparathyroidism is caused by a molecular deletional-insertion involving chromosomes Xq27 and 2p25. by Bowl, MR, Nesbit, M, Harding, B, Levy, E, Schlessinger, D, Whyte, M, Thakker, R

Maturity-onset diabetes of the young caused by a balanced translocation where the 20q12 break point results in disruption upstream of the coding region of hepatocyte nuclear factor... by Gloyn, A, Ellard, S, Shepherd, M, Howell, RT, Parry, E, Jefferson, A, Levy, E, Hattersley, A

Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region by Bonora, E, Bacchelli, E, Levy, E, Blasi, F, Marlow, A, Monaco, A, Maestrini, E, Conso, I

A gene-based genetic linkage and comparative map of the rat X chromosome. by Millwood, I, Bihoreau, M, Gauguier, D, Hyne, G, Levy, E, Kreutz, R, Lathrop, G, Monaco, A

Assignment of genes encoding GABAA receptor subunits alpha 1, alpha 6, beta 2, and gamma 2 to a YAC contig of 5q33. by Kostrzewa, M, Köhler, A, Eppelt, K, Hellam, L, Fairweather, N, Levy, E, Monaco, A, Müller, U

Physical and transcriptional characterization of the commonly deleted region in del(9q) AML. by Daly, S, Wainscoat, J, Side, L, Levy, E, Kusec, R, Kasprzyk, A, Gama, S, Humphray, S, Boultwood, J, Peniket, A